HAND SANITIZER

Manufacturer
SPLENDID KEEN LIMITED
Effective date
2020-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:06

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store between 15°-30°C (59°-89°F),Awold freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT SECTION

ALOE EXTRACT,GLYCERIN, ISOPROPYL ALCOHOL, ISOPROPYL MYRISTATE, POLYACRYLIC ACID, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, WATER

INDICATIONS & USAGE SECTION

Place enough product on your hands to cover all suraces.Rub hands together until dry.

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

For external use only, Flamable. Keep away from heat or flame.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66875-001-012022-01-28C16284748780-1d6a99b39-5b0f-a426-e053-dadaa90af4c2a7ca7bab-d51f-b8c7-e053-2995a90ae62b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66875-001-01HAND SANITIZER60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66875-001HAND SANITIZER GEL [SPLENDID KEEN LIMITED]1Legacy NDC, 1 package rows20200618_a7ca7bab-d51f-b8c7-e053-2995a90ae62b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66875-00166875-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a7ca7bab-d520-b8c7-e053-2995a90ae62ba7ca7bab-d51f-b8c7-e053-2995a90ae62b2020-06-11WarningsExact identifier
spl id: a7ca7bab-d520-b8c7-e053-2995a90ae62b
spl set id: a7ca7bab-d51f-b8c7-e053-2995a90ae62b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.